Allele Registry

Canonical Allele Identifier: PA2825748479

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000592288

RCV001867926

ClinVar Variation:

497674

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Tyr1634Cys	CA347220291 NM_001130976.2:c.4901A>G